Singh Anukriti, Srivastava Nidhi, Amit Sonal, Prasad S N, Misra M P, Ateeq Bushra
Molecular Oncology Lab, Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur, 208016, U.P., India; Department of Bioscience and Biotechnology, Banasthali University, Tonk, 304022, Rajasthan, India.
Department of Bioscience and Biotechnology, Banasthali University, Tonk, 304022, Rajasthan, India.
Transl Oncol. 2018 Apr;11(2):233-242. doi: 10.1016/j.tranon.2017.12.007. Epub 2018 Feb 3.
Renin angiotensin system (RAS) comprising Angiotensin converting enzyme (ACE), Angiotensin II (Ang II) and its receptor Angiotensin II receptor type I (AGTR1), plays a critical role in several diseases including cancer. A single nucleotide polymorphism (SNP) A1166C located in 3' untranslated region (UTR) of AGTR1 and an insertion/deletion (I/D) polymorphism present in intron 16 of ACE gene have been associated with many diseases, but their association with Breast cancer (BCa) is still debatable. Here, we for the first time investigated the association of these polymorphisms in a North Indian BCa cohort including 161 patients and 152 healthy women. The polymorphisms were evaluated by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) respectively. The association between these polymorphisms and BCa risk was estimated by calculating Odds Ratio (OR) and chi-square (χ) test. The DD genotype/D allele of ACE (I/D) polymorphism and "AC and CC" genotype/C allele of AGTR1 (A1166C) polymorphism were associated with higher risk of BCa when evaluated independently. Furthermore, interaction analysis of "AC and CC" and DD genotype and combination of "C and D" alleles of both polymorphisms revealed significantly greater BCa risk than that observed independently. Conclusively, women harboring "AC or CC" genotype/C allele for AGTR1 (A1166C) polymorphism and DD genotype/D allele for ACE (I/D) polymorphisms have a predisposition to develop more aggressive disease with advanced staging and larger tumor size. Our study indicates importance of genetic screening based on these polymorphisms for women, who may have higher risk of BCa.
肾素血管紧张素系统(RAS)由血管紧张素转换酶(ACE)、血管紧张素II(Ang II)及其受体血管紧张素II 1型受体(AGTR1)组成,在包括癌症在内的多种疾病中起关键作用。位于AGTR1基因3'非翻译区(UTR)的单核苷酸多态性(SNP)A1166C以及ACE基因第16内含子中的插入/缺失(I/D)多态性与许多疾病相关,但其与乳腺癌(BCa)的关联仍存在争议。在此,我们首次在一个包括161例患者和152名健康女性的北印度乳腺癌队列中研究了这些多态性的关联。分别通过聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)评估这些多态性。通过计算优势比(OR)和卡方(χ)检验来估计这些多态性与乳腺癌风险之间的关联。单独评估时,ACE(I/D)多态性的DD基因型/D等位基因以及AGTR1(A1166C)多态性的“AC和CC”基因型/C等位基因与更高的乳腺癌风险相关。此外,“AC和CC”与DD基因型以及两种多态性的“C和D”等位基因组合的相互作用分析显示,乳腺癌风险显著高于单独观察到的情况。总之,携带AGTR1(A1166C)多态性的“AC或CC”基因型/C等位基因以及ACE(I/D)多态性的DD基因型/D等位基因的女性易患更具侵袭性疾病,分期更晚且肿瘤更大。我们的研究表明,基于这些多态性对可能具有较高乳腺癌风险的女性进行基因筛查具有重要意义。